GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Stenotrophomonas chelatiphaga DSM 21508

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate WP_057507255.1 ABB28_RS03320 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>NCBI__GCF_001431535.1:WP_057507255.1
          Length = 323

 Score =  438 bits (1127), Expect = e-128
 Identities = 214/316 (67%), Positives = 258/316 (81%), Gaps = 1/316 (0%)

Query: 5   RHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPA 64
           RH +++ILGSGPAG++AAVYAARANLKP++ITG+Q GGQL TTTEVDNWPGD HGL GP 
Sbjct: 8   RHQKLVILGSGPAGWTAAVYAARANLKPVVITGLQQGGQLMTTTEVDNWPGDAHGLMGPD 67

Query: 65  LMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPS 124
           LM RM+ HAERFETE++FDHI+  D + +P+ L GDSA YTCDALII+TGA+A+YLG+PS
Sbjct: 68  LMARMQAHAERFETEVIFDHIHTADLSQRPFKLIGDSAEYTCDALIISTGATAKYLGIPS 127

Query: 125 EEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAE 184
           EE F G+GVSACATCDGFFYR++ V VVGGGNTAVEEALYL+NIA  V L+HRR+T +AE
Sbjct: 128 EETFKGRGVSACATCDGFFYRDQDVVVVGGGNTAVEEALYLSNIARKVYLVHRRDTLKAE 187

Query: 185 KILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKN-NDGSFDELKVDGVFIAIG 243
           KI+ DKL A+VA GKI    +  +DEVLG++ GVTG R+K+  DGS  +++  G F+AIG
Sbjct: 188 KIMQDKLFAKVAAGKIETVWHHQVDEVLGNDAGVTGVRVKSVQDGSTRDIEAHGFFVAIG 247

Query: 244 HTPNTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAGCM 303
           H PNT+LF+GQL +  GYL ++ G  GNAT TSVEG+FAAGDVAD  YRQAITSAG GCM
Sbjct: 248 HHPNTTLFDGQLAMNHGYLEIRSGLGGNATQTSVEGVFAAGDVADQHYRQAITSAGFGCM 307

Query: 304 AALDTERYLDGLQNAS 319
           AALD ERYLD    AS
Sbjct: 308 AALDAERYLDAQGKAS 323


Lambda     K      H
   0.318    0.135    0.386 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 379
Number of extensions: 15
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 320
Length of database: 323
Length adjustment: 28
Effective length of query: 292
Effective length of database: 295
Effective search space:    86140
Effective search space used:    86140
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory